K-number	K770891
Device name	SPLINH, FOREARM
Applicant	Orthopedic Systems, Inc.
Product code	IQM
Device class	Class I
Decision date	May 26, 1977
Decision	Substantially Equivalent
Regulation	890.3025

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View the full FDA submission: accessdata.fda.gov

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SPLINH, FOREARM

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